Canonical Allele Identifier: PA159592
Gene: FANCG HGNC NCBI

Linked Data

ClinVar Variation Id: 134357

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004620.1:p.Gln26Arg
CA159590
NM_004629.2:c.77A>G